Canonical Allele Identifier: PA2573256348
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1349586
ClinVar RCV Id: RCV002047028

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Cys1980Ser
CA384890758
NM_014191.4:c.5938T>A
CA384890762
NM_014191.4:c.5939G>C